Run ID: SRR1140625
Sample name:
Date: 02-04-2023 20:57:06
Number of reads: 2433789
Percentage reads mapped: 93.91
Strain: lineage3
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Ala | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.15 | streptomycin |
katG | 2155700 | p.Asn138His | missense_variant | 1.0 | isoniazid |
embB | 4249518 | p.His1002Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761292 | p.Val496Met | missense_variant | 0.97 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1460914 | c.-131G>T | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472007 | n.162G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473856 | n.199A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474302 | n.645G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475277 | n.1620G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475469 | n.1812C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475479 | n.1822C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475481 | n.1824C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475484 | n.1828delC | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475498 | n.1841C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918067 | p.Ala43Asp | missense_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168605 | p.Pro670Ala | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726117 | c.-76T>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642877 | p.Lys448Arg | missense_variant | 1.0 |
embC | 4240732 | p.Asn290Lys | missense_variant | 0.13 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.97 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |